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Electromyographic evaluation of the effect of pelvic floor muscle training to improve the function of the lower urinary tract in women with ischemic stroke

Electromyographic evaluation of the effect of pelvic floor muscle training to improve the function of the lower urinary tract in women with ischemic stroke: a prospective, randomized study with a control group.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617000162314
Enrollment
40
Registered
2017-01-30
Start date
2017-02-20
Completion date
Unknown
Last updated
2017-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The primary objective of the study is electromyographic assessment of the impact of pelvic floor muscle training (MDM) to improve the function of the lower urinary tract in women after ischemic stroke. The research will be carried out in the Department of Neurological Rehabilitation in Regional Hospital in Wroclaw. Participants in the study will be randomized to one of two comparison groups: group A - group, which will be used PFM training and group B (control) - a group without specialized training of PFM. All patients will be performed evaluation parameters included in the project at the beginning of your stay in the hospital after ten days (in group A after ten days of treatment) and after 20 days (follow up). Resting and functional bioelectric activity of PFM will be assessed by the electromyographic device MyoSystem 1400L.

Interventions

Participants will be randomly assigned to one of two comparison groups: A group - group, which will be used pelvic floor muscle training and B group (control) - a group without specialized training of the pelvic floor muscles. In group A will be applied the pelvic floor muscle training. Therapy will be held for ten days (two weeks at five sessions per week) and each will last about 30 minutes a day. The whole therapy will be carried out under the supervision of a therapist at the hospital. Parti

Participants will be randomly assigned to one of two comparison groups: A group - group, which will be used pelvic floor muscle training and B group (control) - a group without specialized training of the pelvic floor muscles. In group A will be applied the pelvic floor muscle training. Therapy will be held for ten days (two weeks at five sessions per week) and each will last about 30 minutes a day. The whole therapy will be carried out under the supervision of a therapist at the hospital. Participants will be recruited from among patients of the hospital Selection of exercises will be individual determined, in depends on the function of the lower urinary tract and the condition of the tested women (physiotherapist decision). Training will take into account the contractions of the pelvic floor muscles. Participants will perform contraction lasting a few seconds (depending on the condition of the patient, with a break lasts twice as long). They will also be carried out short, rapid contraction of this muscle. In this training, a electromyograph with the function of the visual biofeedback will be used. Feedback on muscle contraction provided via a screen for participants throughout each session via sEMG sensors. Each training session will be supervised and managed by a physiotherapist.

Sponsors

Wroclaw Medical University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

ischaemic stroke episode for at least 6 months previously, the incidence of symptoms of lower urinary tract (urinary incontinence), consent to participate in research, permission doctor and general well-being of the survey

Exclusion criteria

aphasia sensory, significant abdominal obesity (BMI> 30), previous surgery within the abdominal wall and / or pelvic, people with limited abilities functional (Barthel index <60), age over 75 years, incontinence grade III, fecal incontinence, gynecological surgeries, the lack of consent of the person tested and the lack of consent doctor to perform measurements, malaise on the study, contraindications measurements - infection, menstruation, allergic to nickel, the occurrence of pain during the study period, the resignation during the study

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026